Cresilon, Inc.

Cresilon, Inc. — FDA 510(k) Submissions

Cresilon, Inc. has submitted 3 FDA 510(k) premarket notifications since 2023, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Hemostatic Wound Dressing Without Thrombin Or Other Biologics . Use the specialty filter in the sidebar to narrow results.